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Artigo de periodico
Aplicação de ferramentas pedagógicas na disciplina de Química Orgânica I de forma remota (2023)
Damada, Pedro Henrique ; Porto, Andre Luiz Meleiro
Source: Quimica Nova na Escola. Unidade: IQSC
Subjects: ENSINO SUPERIOR, QUÍMICA ORGÂNICA, DIVULGAÇÃO CIENTÍFICA
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ABNT
DAMADA, Pedro Henrique e PORTO, Andre Luiz Meleiro. Aplicação de ferramentas pedagógicas na disciplina de Química Orgânica I de forma remota. Quimica Nova na Escola, n. 1, p. 20-29, 2023Tradução . . Disponível em: https://doi.org/10.21577/0104-8899.20160289. Acesso em: 09 nov. 2024.
APA
Damada, P. H., & Porto, A. L. M. (2023). Aplicação de ferramentas pedagógicas na disciplina de Química Orgânica I de forma remota. Quimica Nova na Escola, ( 1), 20-29. doi:10.21577/0104-8899.20160289
NLM
Damada PH, Porto ALM. Aplicação de ferramentas pedagógicas na disciplina de Química Orgânica I de forma remota [Internet]. Quimica Nova na Escola. 2023 ;( 1): 20-29.[citado 2024 nov. 09 ] Available from: https://doi.org/10.21577/0104-8899.20160289
Vancouver
Damada PH, Porto ALM. Aplicação de ferramentas pedagógicas na disciplina de Química Orgânica I de forma remota [Internet]. Quimica Nova na Escola. 2023 ;( 1): 20-29.[citado 2024 nov. 09 ] Available from: https://doi.org/10.21577/0104-8899.20160289
Artigo de periodico
Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network (2021)
Khalid, Muhammad ; Ali, Akbar ; Khan, Muhammad Usman ; Tahir, Muhammad Nawaz; Ahmad, Anees ; Ashfaq, Muhammad; Hussain, Riaz; Morais, Sara Figueirêdo de Alcântara ; Braga, Ataualpa Albert Carmo
Source: Journal of Molecular Structure. Unidades: IQ, IQSC
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
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ABNT
KHALID, Muhammad et al. Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network. Journal of Molecular Structure, v. 1230 p. 129827, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2020.129827. Acesso em: 09 nov. 2024.
APA
Khalid, M., Ali, A., Khan, M. U., Tahir, M. N., Ahmad, A., Ashfaq, M., et al. (2021). Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network. Journal of Molecular Structure, 1230 p. 129827. doi:10.1016/j.molstruc.2020.129827
NLM
Khalid M, Ali A, Khan MU, Tahir MN, Ahmad A, Ashfaq M, Hussain R, Morais SF de A, Braga AAC. Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network [Internet]. Journal of Molecular Structure. 2021 ; 1230 p. 129827[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129827
Vancouver
Khalid M, Ali A, Khan MU, Tahir MN, Ahmad A, Ashfaq M, Hussain R, Morais SF de A, Braga AAC. Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network [Internet]. Journal of Molecular Structure. 2021 ; 1230 p. 129827[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129827
Artigo de periodico
A simple, rapid, green and non-destructive 19F time-domain NMR method for directly fluorine determination in powder of mineral supplements for cattle (2020)
Babos, Diego Victor ; Garcia, Rodrigo Henrique dos Santos ; Colnago, Luiz Alberto ; Pereira Filho, Edenir Rodrigues
Source: Microchemical Journal. Unidade: IQSC
Subjects: QUÍMICA ORGÂNICA, NUTRIENTES PARA ANIMAIS, FLÚOR
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ABNT
BABOS, Diego Victor et al. A simple, rapid, green and non-destructive 19F time-domain NMR method for directly fluorine determination in powder of mineral supplements for cattle. Microchemical Journal, v. 153, p. 104416, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.microc.2019.104416. Acesso em: 09 nov. 2024.
APA
Babos, D. V., Garcia, R. H. dos S., Colnago, L. A., & Pereira Filho, E. R. (2020). A simple, rapid, green and non-destructive 19F time-domain NMR method for directly fluorine determination in powder of mineral supplements for cattle. Microchemical Journal, 153, 104416. doi:10.1016/j.microc.2019.104416
NLM
Babos DV, Garcia RH dos S, Colnago LA, Pereira Filho ER. A simple, rapid, green and non-destructive 19F time-domain NMR method for directly fluorine determination in powder of mineral supplements for cattle [Internet]. Microchemical Journal. 2020 ; 153 104416.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.microc.2019.104416
Vancouver
Babos DV, Garcia RH dos S, Colnago LA, Pereira Filho ER. A simple, rapid, green and non-destructive 19F time-domain NMR method for directly fluorine determination in powder of mineral supplements for cattle [Internet]. Microchemical Journal. 2020 ; 153 104416.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.microc.2019.104416
Artigo de periodico
α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles (2020)
Caiuby, Clarice Alves Dale ; Jesus, Matheus Pereira de ; Burtoloso, Antonio Carlos Bender
Source: The Journal of Organic Chemistry. Unidade: IQSC
Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
CAIUBY, Clarice Alves Dale e JESUS, Matheus Pereira de e BURTOLOSO, Antonio Carlos Bender. α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles. The Journal of Organic Chemistry, v. 85, n. 11, p. 7433-7445 April 28, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.0c00833. Acesso em: 09 nov. 2024.
APA
Caiuby, C. A. D., Jesus, M. P. de, & Burtoloso, A. C. B. (2020). α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles. The Journal of Organic Chemistry, 85( 11), 7433-7445 April 28. doi:10.1021/acs.joc.0c00833
NLM
Caiuby CAD, Jesus MP de, Burtoloso ACB. α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles [Internet]. The Journal of Organic Chemistry. 2020 ;85( 11): 7433-7445 April 28.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1021/acs.joc.0c00833
Vancouver
Caiuby CAD, Jesus MP de, Burtoloso ACB. α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles [Internet]. The Journal of Organic Chemistry. 2020 ;85( 11): 7433-7445 April 28.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1021/acs.joc.0c00833
Artigo de periodico
Studying the catecholamine effect on the electronic delocalization of the paramagnetic [Ru(NH3)4(catecholamine)]+ complex through 1H-NMR, theoretical calculations, and resonance Raman (2020)
Alves, Jacqueline Q.; Formiga, André L. B.; Gonçalves, Rogéria Rocha ; Silva, Roberto Santana da
Source: Journal of Coordination Chemistry. Unidades: FFCLRP, FCFRP
Subjects: RUTÊNIO, QUÍMICA ORGÂNICA, CATECOLAMINAS
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ABNT
ALVES, Jacqueline Q. et al. Studying the catecholamine effect on the electronic delocalization of the paramagnetic [Ru(NH3)4(catecholamine)]+ complex through 1H-NMR, theoretical calculations, and resonance Raman. Journal of Coordination Chemistry, v. 73, n. 2, p. 191-205, 2020Tradução . . Disponível em: https://doi.org/10.1080/00958972.2020.1724287. Acesso em: 09 nov. 2024.
APA
Alves, J. Q., Formiga, A. L. B., Gonçalves, R. R., & Silva, R. S. da. (2020). Studying the catecholamine effect on the electronic delocalization of the paramagnetic [Ru(NH3)4(catecholamine)]+ complex through 1H-NMR, theoretical calculations, and resonance Raman. Journal of Coordination Chemistry, 73( 2), 191-205. doi:10.1080/00958972.2020.1724287
NLM
Alves JQ, Formiga ALB, Gonçalves RR, Silva RS da. Studying the catecholamine effect on the electronic delocalization of the paramagnetic [Ru(NH3)4(catecholamine)]+ complex through 1H-NMR, theoretical calculations, and resonance Raman [Internet]. Journal of Coordination Chemistry. 2020 ; 73( 2): 191-205.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1080/00958972.2020.1724287
Vancouver
Alves JQ, Formiga ALB, Gonçalves RR, Silva RS da. Studying the catecholamine effect on the electronic delocalization of the paramagnetic [Ru(NH3)4(catecholamine)]+ complex through 1H-NMR, theoretical calculations, and resonance Raman [Internet]. Journal of Coordination Chemistry. 2020 ; 73( 2): 191-205.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1080/00958972.2020.1724287
Artigo de periodico
Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides (2019)
Ahmad, Anees; Burtoloso, Antonio Carlos Bender
Source: Organic letters. Unidade: IQSC
Assunto: QUÍMICA ORGÂNICA
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ABNT
AHMAD, Anees e BURTOLOSO, Antonio Carlos Bender. Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides. Organic letters, v. 21, p. 6079-6083, 2019Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.9b02221. Acesso em: 09 nov. 2024.
APA
Ahmad, A., & Burtoloso, A. C. B. (2019). Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides. Organic letters, 21, 6079-6083. doi:10.1021/acs.orglett.9b02221
NLM
Ahmad A, Burtoloso ACB. Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides [Internet]. Organic letters. 2019 ;21 6079-6083.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1021/acs.orglett.9b02221
Vancouver
Ahmad A, Burtoloso ACB. Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides [Internet]. Organic letters. 2019 ;21 6079-6083.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1021/acs.orglett.9b02221
Artigo de periodico
Metal-free Insertion Reactions of Diazo carbonyls to Azlactones (2018)
Mello,Amanda C.; Momo, Patrícia Betoni; Burtoloso, Antonio Carlos Bender ; Amarante, Giovanni W
Source: The Journal of Organic Chemistry. Unidade: IQSC
Assunto: QUÍMICA ORGÂNICA
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ABNT
MELLO, Amanda C. et al. Metal-free Insertion Reactions of Diazo carbonyls to Azlactones. The Journal of Organic Chemistry, v. 83, p. 11399-11406, 2018Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.8b01683. Acesso em: 09 nov. 2024.
APA
Mello, A. C., Momo, P. B., Burtoloso, A. C. B., & Amarante, G. W. (2018). Metal-free Insertion Reactions of Diazo carbonyls to Azlactones. The Journal of Organic Chemistry, 83, 11399-11406. doi:10.1021/acs.joc.8b01683
NLM
Mello AC, Momo PB, Burtoloso ACB, Amarante GW. Metal-free Insertion Reactions of Diazo carbonyls to Azlactones [Internet]. The Journal of Organic Chemistry. 2018 ;83 11399-11406.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1021/acs.joc.8b01683
Vancouver
Mello AC, Momo PB, Burtoloso ACB, Amarante GW. Metal-free Insertion Reactions of Diazo carbonyls to Azlactones [Internet]. The Journal of Organic Chemistry. 2018 ;83 11399-11406.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1021/acs.joc.8b01683
Artigo de periodico
Coupling of sulfoxonium ylides with arynes: a direct synthesis of pro-chiral aryl ketosulfoxonium ylides and its application in the preparation of α‑aryl ketones (2018)
Talero, Alexánder G; Martins, Bruna S; Burtoloso, Antonio Carlos Bender
Source: Organic letters. Unidade: IQSC
Assunto: QUÍMICA ORGÂNICA
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ABNT
TALERO, Alexánder G e MARTINS, Bruna S e BURTOLOSO, Antonio Carlos Bender. Coupling of sulfoxonium ylides with arynes: a direct synthesis of pro-chiral aryl ketosulfoxonium ylides and its application in the preparation of α‑aryl ketones. Organic letters, v. 20, p. 7206-7211, 2018Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.8b03126. Acesso em: 09 nov. 2024.
APA
Talero, A. G., Martins, B. S., & Burtoloso, A. C. B. (2018). Coupling of sulfoxonium ylides with arynes: a direct synthesis of pro-chiral aryl ketosulfoxonium ylides and its application in the preparation of α‑aryl ketones. Organic letters, 20, 7206-7211. doi:10.1021/acs.orglett.8b03126
NLM
Talero AG, Martins BS, Burtoloso ACB. Coupling of sulfoxonium ylides with arynes: a direct synthesis of pro-chiral aryl ketosulfoxonium ylides and its application in the preparation of α‑aryl ketones [Internet]. Organic letters. 2018 ;20 7206-7211.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1021/acs.orglett.8b03126
Vancouver
Talero AG, Martins BS, Burtoloso ACB. Coupling of sulfoxonium ylides with arynes: a direct synthesis of pro-chiral aryl ketosulfoxonium ylides and its application in the preparation of α‑aryl ketones [Internet]. Organic letters. 2018 ;20 7206-7211.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1021/acs.orglett.8b03126
Artigo de periodico
Silica-supported HClO4 promotes catalytic solvent- and metal-free O-H insertion reactions with diazo compounds (2018)
Gallo, Rafael D. C; Burtoloso, Antonio Carlos Bender
Source: Green Chemistry. Unidade: IQSC
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
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ABNT
GALLO, Rafael D. C e BURTOLOSO, Antonio Carlos Bender. Silica-supported HClO4 promotes catalytic solvent- and metal-free O-H insertion reactions with diazo compounds. Green Chemistry, v. 20, p. 4547-4556, 2018Tradução . . Disponível em: https://doi.org/10.1039/C8GC02574F. Acesso em: 09 nov. 2024.
APA
Gallo, R. D. C., & Burtoloso, A. C. B. (2018). Silica-supported HClO4 promotes catalytic solvent- and metal-free O-H insertion reactions with diazo compounds. Green Chemistry, 20, 4547-4556. doi:10.1039/C8GC02574F
NLM
Gallo RDC, Burtoloso ACB. Silica-supported HClO4 promotes catalytic solvent- and metal-free O-H insertion reactions with diazo compounds [Internet]. Green Chemistry. 2018 ;20 4547-4556.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1039/C8GC02574F
Vancouver
Gallo RDC, Burtoloso ACB. Silica-supported HClO4 promotes catalytic solvent- and metal-free O-H insertion reactions with diazo compounds [Internet]. Green Chemistry. 2018 ;20 4547-4556.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1039/C8GC02574F
Artigo de periodico
A combined approach using differential scanning calorimetry with polarized light thermomicroscopy in the investigation of ketoprofen and nicotinamide cocrystal (2017)
Perpétuo, Glauco Lini; Chierice, Gilberto Orivaldo; Ferreira, L T; Frga-Silva, T. F. C.; Venturini, James; Arruda, M. S. P.; Bannach, G; Castro, R.A.E.
Source: Thermochimica Acta. Unidade: IQSC
Assunto: QUÍMICA ORGÂNICA
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ABNT
PERPÉTUO, Glauco Lini et al. A combined approach using differential scanning calorimetry with polarized light thermomicroscopy in the investigation of ketoprofen and nicotinamide cocrystal. Thermochimica Acta, v. 651, p. 1-10, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tca.2017.02.014. Acesso em: 09 nov. 2024.
APA
Perpétuo, G. L., Chierice, G. O., Ferreira, L. T., Frga-Silva, T. F. C., Venturini, J., Arruda, M. S. P., et al. (2017). A combined approach using differential scanning calorimetry with polarized light thermomicroscopy in the investigation of ketoprofen and nicotinamide cocrystal. Thermochimica Acta, 651, 1-10. doi:10.1016/j.tca.2017.02.014
NLM
Perpétuo GL, Chierice GO, Ferreira LT, Frga-Silva TFC, Venturini J, Arruda MSP, Bannach G, Castro RAE. A combined approach using differential scanning calorimetry with polarized light thermomicroscopy in the investigation of ketoprofen and nicotinamide cocrystal [Internet]. Thermochimica Acta. 2017 ;651 1-10.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.tca.2017.02.014
Vancouver
Perpétuo GL, Chierice GO, Ferreira LT, Frga-Silva TFC, Venturini J, Arruda MSP, Bannach G, Castro RAE. A combined approach using differential scanning calorimetry with polarized light thermomicroscopy in the investigation of ketoprofen and nicotinamide cocrystal [Internet]. Thermochimica Acta. 2017 ;651 1-10.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.tca.2017.02.014
Artigo de periodico
Palladium-mediated catalysis leads to intramolecular narcissistic self-sorting on a cavitand platform (2017)
Nagymihaly, Zoltan; Caturello, Naidel A. M. S.; Takatsy, Aniko; Aragay, Gemm; Kollar, Laszlo; Albuquerque, Rodrigo Queiroz de; Csok, Zsolt
Source: Journal of Organic Chemistry. Unidade: IQSC
Assunto: QUÍMICA ORGÂNICA
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ABNT
NAGYMIHALY, Zoltan et al. Palladium-mediated catalysis leads to intramolecular narcissistic self-sorting on a cavitand platform. Journal of Organic Chemistry, v. 82, n. 1, 2017Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.6b02472. Acesso em: 09 nov. 2024.
APA
Nagymihaly, Z., Caturello, N. A. M. S., Takatsy, A., Aragay, G., Kollar, L., Albuquerque, R. Q. de, & Csok, Z. (2017). Palladium-mediated catalysis leads to intramolecular narcissistic self-sorting on a cavitand platform. Journal of Organic Chemistry, 82( 1). doi:10.1021/acs.joc.6b02472
NLM
Nagymihaly Z, Caturello NAMS, Takatsy A, Aragay G, Kollar L, Albuquerque RQ de, Csok Z. Palladium-mediated catalysis leads to intramolecular narcissistic self-sorting on a cavitand platform [Internet]. Journal of Organic Chemistry. 2017 ; 82( 1):[citado 2024 nov. 09 ] Available from: https://doi.org/10.1021/acs.joc.6b02472
Vancouver
Nagymihaly Z, Caturello NAMS, Takatsy A, Aragay G, Kollar L, Albuquerque RQ de, Csok Z. Palladium-mediated catalysis leads to intramolecular narcissistic self-sorting on a cavitand platform [Internet]. Journal of Organic Chemistry. 2017 ; 82( 1):[citado 2024 nov. 09 ] Available from: https://doi.org/10.1021/acs.joc.6b02472
Artigo de periodico
First Asymmetric Reduction of Isatin by Marine-Derived Fungi (2017)
Birolli, Willian Garcia; Ferreira, Irlon Maciel; Jimenez, David Esteban Quintero; Silva, Bianca N. M.; Silva, Bárbara V.; Pinto, Angelo C; Porto, Andre Luiz Meleiro
Source: Journal of the Brazilian Chemical Society. Unidade: IQSC
Assunto: QUÍMICA ORGÂNICA
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ABNT
BIROLLI, Willian Garcia et al. First Asymmetric Reduction of Isatin by Marine-Derived Fungi. Journal of the Brazilian Chemical Society, v. 28, n. 6, p. 1023-1029, 2017Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20160256. Acesso em: 09 nov. 2024.
APA
Birolli, W. G., Ferreira, I. M., Jimenez, D. E. Q., Silva, B. N. M., Silva, B. V., Pinto, A. C., & Porto, A. L. M. (2017). First Asymmetric Reduction of Isatin by Marine-Derived Fungi. Journal of the Brazilian Chemical Society, 28( 6), 1023-1029. doi:10.21577/0103-5053.20160256
NLM
Birolli WG, Ferreira IM, Jimenez DEQ, Silva BNM, Silva BV, Pinto AC, Porto ALM. First Asymmetric Reduction of Isatin by Marine-Derived Fungi [Internet]. Journal of the Brazilian Chemical Society. 2017 ; 28( 6): 1023-1029.[citado 2024 nov. 09 ] Available from: https://doi.org/10.21577/0103-5053.20160256
Vancouver
Birolli WG, Ferreira IM, Jimenez DEQ, Silva BNM, Silva BV, Pinto AC, Porto ALM. First Asymmetric Reduction of Isatin by Marine-Derived Fungi [Internet]. Journal of the Brazilian Chemical Society. 2017 ; 28( 6): 1023-1029.[citado 2024 nov. 09 ] Available from: https://doi.org/10.21577/0103-5053.20160256
Artigo de periodico
Biocatalytic production of chiral benzotriazoles employing conventional heating and microwave radiation (2017)
Meirelles, Matheus Andrade; Jeller, Alex H.; Ferreira, Irlon Maciel; Raminelli, Cristiano; Faria, Raquel S.; Silveira-Lacerda, Elisângela de Paula; Porto, Andre Luiz Meleiro
Source: Current Microwave Chemistry. Unidade: IQSC
Subjects: BENZENO, QUÍMICA ORGÂNICA
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ABNT
MEIRELLES, Matheus Andrade et al. Biocatalytic production of chiral benzotriazoles employing conventional heating and microwave radiation. Current Microwave Chemistry, v. 4, p. 1-4 + supl. 1-17, 2017Tradução . . Disponível em: https://doi.org/10.2174/2213335603666161101152243. Acesso em: 09 nov. 2024.
APA
Meirelles, M. A., Jeller, A. H., Ferreira, I. M., Raminelli, C., Faria, R. S., Silveira-Lacerda, E. de P., & Porto, A. L. M. (2017). Biocatalytic production of chiral benzotriazoles employing conventional heating and microwave radiation. Current Microwave Chemistry, 4, 1-4 + supl. 1-17. doi:10.2174/2213335603666161101152243
NLM
Meirelles MA, Jeller AH, Ferreira IM, Raminelli C, Faria RS, Silveira-Lacerda E de P, Porto ALM. Biocatalytic production of chiral benzotriazoles employing conventional heating and microwave radiation [Internet]. Current Microwave Chemistry. 2017 ; 4 1-4 + supl. 1-17.[citado 2024 nov. 09 ] Available from: https://doi.org/10.2174/2213335603666161101152243
Vancouver
Meirelles MA, Jeller AH, Ferreira IM, Raminelli C, Faria RS, Silveira-Lacerda E de P, Porto ALM. Biocatalytic production of chiral benzotriazoles employing conventional heating and microwave radiation [Internet]. Current Microwave Chemistry. 2017 ; 4 1-4 + supl. 1-17.[citado 2024 nov. 09 ] Available from: https://doi.org/10.2174/2213335603666161101152243
Artigo de periodico
Towards low-cost bioanalytical tools for sarcosine assays for cancer diagnostics (2016)
Mazzu Nascimento, Thiago; Leão, Paulo Augusto Gomes Carneiro; Catai, Jonatan Ricardo; Morbioli, Giorgio Gianini; Carrilho, Emanuel
Source: Analytical Methods. Unidade: IQSC
Subjects: AMINOÁCIDOS, QUÍMICA ORGÂNICA
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ABNT
MAZZU NASCIMENTO, Thiago et al. Towards low-cost bioanalytical tools for sarcosine assays for cancer diagnostics. Analytical Methods, v. 8, n. 40, p. 7312-7318, 2016Tradução . . Disponível em: https://doi.org/10.1039/C6AY01848C. Acesso em: 09 nov. 2024.
APA
Mazzu Nascimento, T., Leão, P. A. G. C., Catai, J. R., Morbioli, G. G., & Carrilho, E. (2016). Towards low-cost bioanalytical tools for sarcosine assays for cancer diagnostics. Analytical Methods, 8( 40), 7312-7318. doi:10.1039/C6AY01848C
NLM
Mazzu Nascimento T, Leão PAGC, Catai JR, Morbioli GG, Carrilho E. Towards low-cost bioanalytical tools for sarcosine assays for cancer diagnostics [Internet]. Analytical Methods. 2016 ; 8( 40): 7312-7318.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1039/C6AY01848C
Vancouver
Mazzu Nascimento T, Leão PAGC, Catai JR, Morbioli GG, Carrilho E. Towards low-cost bioanalytical tools for sarcosine assays for cancer diagnostics [Internet]. Analytical Methods. 2016 ; 8( 40): 7312-7318.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1039/C6AY01848C
Artigo de periodico
Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives (2016)
Fumagalli, Fernando; Emery, Flavio da Silva
Source: The Journal of Organic Chemistry. Unidade: FCFRP
Subjects: QUÍMICA ORGÂNICA, REAÇÕES ORGÂNICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FUMAGALLI, Fernando e EMERY, Flavio da Silva. Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives. The Journal of Organic Chemistry, v. 81, n. 21, p. 10339-10347, 2016Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.6b01329. Acesso em: 09 nov. 2024.
APA
Fumagalli, F., & Emery, F. da S. (2016). Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives. The Journal of Organic Chemistry, 81( 21), 10339-10347. doi:10.1021/acs.joc.6b01329
NLM
Fumagalli F, Emery F da S. Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives [Internet]. The Journal of Organic Chemistry. 2016 ; 81( 21): 10339-10347.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1021/acs.joc.6b01329
Vancouver
Fumagalli F, Emery F da S. Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives [Internet]. The Journal of Organic Chemistry. 2016 ; 81( 21): 10339-10347.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1021/acs.joc.6b01329
Artigo de periodico
Sodium lignosulfonate as a renewable stabilizing agent for aqueous alumina suspensions (2016)
Megiatto Junior, Jackson Dirceu; Cerrutti, Bianca Machado; Frollini, Elisabete
Source: International Journal of Biological Macromolecules. Unidade: IQSC
Assunto: QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MEGIATTO JUNIOR, Jackson Dirceu e CERRUTTI, Bianca Machado e FROLLINI, Elisabete. Sodium lignosulfonate as a renewable stabilizing agent for aqueous alumina suspensions. International Journal of Biological Macromolecules, v. 82, p. 927-932, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.ijbiomac.2015.11.004. Acesso em: 09 nov. 2024.
APA
Megiatto Junior, J. D., Cerrutti, B. M., & Frollini, E. (2016). Sodium lignosulfonate as a renewable stabilizing agent for aqueous alumina suspensions. International Journal of Biological Macromolecules, 82, 927-932. doi:10.1016/j.ijbiomac.2015.11.004
NLM
Megiatto Junior JD, Cerrutti BM, Frollini E. Sodium lignosulfonate as a renewable stabilizing agent for aqueous alumina suspensions [Internet]. International Journal of Biological Macromolecules. 2016 ; 82 927-932.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.ijbiomac.2015.11.004
Vancouver
Megiatto Junior JD, Cerrutti BM, Frollini E. Sodium lignosulfonate as a renewable stabilizing agent for aqueous alumina suspensions [Internet]. International Journal of Biological Macromolecules. 2016 ; 82 927-932.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.ijbiomac.2015.11.004
Artigo de periodico
Stoichiometric and irreversible cysteine-selective protein modification using carbonylacrylic reagents (2016)
Bernardim, Barbara; Cal, Pedro M. S. D.; Matos, Maria J.; Oliveira, Bruno L.; Martínez-Sáez, Nuria; Albuquerque, Inês S; Perkins, Elizabeth; Corzana, Francisco; Burtoloso, Antonio Carlos Bender ; Jiménez-Osés, Gonzalo; Bernardes, Gonçalo L. L.
Source: Nature Communications. Unidade: IQSC
Subjects: QUÍMICA ORGÂNICA, PROTEÍNAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERNARDIM, Barbara et al. Stoichiometric and irreversible cysteine-selective protein modification using carbonylacrylic reagents. Nature Communications, 2016Tradução . . Disponível em: https://doi.org/10.1038/ncomms13128. Acesso em: 09 nov. 2024.
APA
Bernardim, B., Cal, P. M. S. D., Matos, M. J., Oliveira, B. L., Martínez-Sáez, N., Albuquerque, I. S., et al. (2016). Stoichiometric and irreversible cysteine-selective protein modification using carbonylacrylic reagents. Nature Communications. doi:10.1038/ncomms13128
NLM
Bernardim B, Cal PMSD, Matos MJ, Oliveira BL, Martínez-Sáez N, Albuquerque IS, Perkins E, Corzana F, Burtoloso ACB, Jiménez-Osés G, Bernardes GLL. Stoichiometric and irreversible cysteine-selective protein modification using carbonylacrylic reagents [Internet]. Nature Communications. 2016 ;[citado 2024 nov. 09 ] Available from: https://doi.org/10.1038/ncomms13128
Vancouver
Bernardim B, Cal PMSD, Matos MJ, Oliveira BL, Martínez-Sáez N, Albuquerque IS, Perkins E, Corzana F, Burtoloso ACB, Jiménez-Osés G, Bernardes GLL. Stoichiometric and irreversible cysteine-selective protein modification using carbonylacrylic reagents [Internet]. Nature Communications. 2016 ;[citado 2024 nov. 09 ] Available from: https://doi.org/10.1038/ncomms13128
Artigo de periodico
Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186 (2016)
Jimenez, David Esteban Quintero; Ferreira , Irlon Maciel; Birolli, Willian Garcia; Fonseca, Luis P.; Porto, Andre Luiz Meleiro
Source: Tetrahedron. Unidade: IQSC
Subjects: FUNGOS, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JIMENEZ, David Esteban Quintero et al. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186. Tetrahedron, v. 72, n. 46, p. 7317-7322, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2016.02.014. Acesso em: 09 nov. 2024.
APA
Jimenez, D. E. Q., Ferreira , I. M., Birolli, W. G., Fonseca, L. P., & Porto, A. L. M. (2016). Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186. Tetrahedron, 72( 46), 7317-7322. doi:10.1016/j.tet.2016.02.014
NLM
Jimenez DEQ, Ferreira IM, Birolli WG, Fonseca LP, Porto ALM. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186 [Internet]. Tetrahedron. 2016 ; 72( 46): 7317-7322.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.tet.2016.02.014
Vancouver
Jimenez DEQ, Ferreira IM, Birolli WG, Fonseca LP, Porto ALM. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186 [Internet]. Tetrahedron. 2016 ; 72( 46): 7317-7322.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.tet.2016.02.014
Artigo de periodico
Condensation of macrocyclic polyketides produced by penicullium sp.DRF2 with mercaptopyruvate represents a new fungal detoxification pathway (2016)
Castro, Marcos V; Ióca, Laura Pavan ; Williams, David E ; Costa, Bruna Z.; Mizuno, Carolina Megumi; Santos, Mario F. C ; Jesus, Karen de; Ferreira, Everton Lucena F; Seleghim, Mirna Helena Regali ; Sette, Lara Durães ; Pereira Filho, Edenir Rodrigues ; Ferreira, Antonio G; Gonçalves, Natália S.; Santos, Raquel A.; Patrick, Brian O; Andersen, Raymond J ; Berlinck, Roberto Gomes de Souza
Source: Journal of Natural Products. Unidade: IQSC
Subjects: QUÍMICA ORGÂNICA, BIOLOGIA MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTRO, Marcos V et al. Condensation of macrocyclic polyketides produced by penicullium sp.DRF2 with mercaptopyruvate represents a new fungal detoxification pathway. Journal of Natural Products, v. 79, n. 6, p. 1668-1678, 2016Tradução . . Disponível em: https://doi.org/10.1021/acs.jnatprod.6b00295. Acesso em: 09 nov. 2024.
APA
Castro, M. V., Ióca, L. P., Williams, D. E., Costa, B. Z., Mizuno, C. M., Santos, M. F. C., et al. (2016). Condensation of macrocyclic polyketides produced by penicullium sp.DRF2 with mercaptopyruvate represents a new fungal detoxification pathway. Journal of Natural Products, 79( 6), 1668-1678. doi:10.1021/acs.jnatprod.6b00295
NLM
Castro MV, Ióca LP, Williams DE, Costa BZ, Mizuno CM, Santos MFC, Jesus K de, Ferreira ELF, Seleghim MHR, Sette LD, Pereira Filho ER, Ferreira AG, Gonçalves NS, Santos RA, Patrick BO, Andersen RJ, Berlinck RG de S. Condensation of macrocyclic polyketides produced by penicullium sp.DRF2 with mercaptopyruvate represents a new fungal detoxification pathway [Internet]. Journal of Natural Products. 2016 ; 79( 6): 1668-1678.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1021/acs.jnatprod.6b00295
Vancouver
Castro MV, Ióca LP, Williams DE, Costa BZ, Mizuno CM, Santos MFC, Jesus K de, Ferreira ELF, Seleghim MHR, Sette LD, Pereira Filho ER, Ferreira AG, Gonçalves NS, Santos RA, Patrick BO, Andersen RJ, Berlinck RG de S. Condensation of macrocyclic polyketides produced by penicullium sp.DRF2 with mercaptopyruvate represents a new fungal detoxification pathway [Internet]. Journal of Natural Products. 2016 ; 79( 6): 1668-1678.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1021/acs.jnatprod.6b00295
Artigo de periodico
New approach to the synthesis of the natural product aripuanin (2015)
Lazaro, Aline S; Ribeiro, Pedro H. Zana; Sairre, Mirela I; Donate, Paulo Marcos
Source: Synthetic Communications. Unidade: FFCLRP
Subjects: PRODUTOS NATURAIS (SÍNTESE QUÍMICA), SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LAZARO, Aline S et al. New approach to the synthesis of the natural product aripuanin. Synthetic Communications, v. 45, n. 11, p. 1374-1378, 2015Tradução . . Disponível em: https://doi.org/10.1080/00397911.2015.1021426. Acesso em: 09 nov. 2024.
APA
Lazaro, A. S., Ribeiro, P. H. Z., Sairre, M. I., & Donate, P. M. (2015). New approach to the synthesis of the natural product aripuanin. Synthetic Communications, 45( 11), 1374-1378. doi:10.1080/00397911.2015.1021426
NLM
Lazaro AS, Ribeiro PHZ, Sairre MI, Donate PM. New approach to the synthesis of the natural product aripuanin [Internet]. Synthetic Communications. 2015 ; 45( 11): 1374-1378.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1080/00397911.2015.1021426
Vancouver
Lazaro AS, Ribeiro PHZ, Sairre MI, Donate PM. New approach to the synthesis of the natural product aripuanin [Internet]. Synthetic Communications. 2015 ; 45( 11): 1374-1378.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1080/00397911.2015.1021426

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